rs4466998
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4466998(A;A) |
| Make rs4466998(A;C) |
| Make rs4466998(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 65008822 |
| Gene | CHURC1-FNTB, FNTB, MAX |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4466998 |
| dbSNP (classic) | rs4466998 |
| ClinGen | rs4466998 |
| ebi | rs4466998 |
| HLI | rs4466998 |
| Exac | rs4466998 |
| Gnomad | rs4466998 |
| Varsome | rs4466998 |
| LitVar | rs4466998 |
| Map | rs4466998 |
| PheGenI | rs4466998 |
| Biobank | rs4466998 |
| 1000 genomes | rs4466998 |
| hgdp | rs4466998 |
| ensembl | rs4466998 |
| geneview | rs4466998 |
| scholar | rs4466998 |
| rs4466998 | |
| pharmgkb | rs4466998 |
| gwascentral | rs4466998 |
| openSNP | rs4466998 |
| 23andMe | rs4466998 |
| SNPshot | rs4466998 |
| SNPdbe | rs4466998 |
| MSV3d | rs4466998 |
| GWAS Ctlg | rs4466998 |
| GMAF | 0.4417 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19862010 ]
|
| Trait | Mean corpuscular volume |
| Title | Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium |
| Risk Allele | A |
| P-val | 5E-8 |
| Odds Ratio | 0 [0.001-0.003] fl increase |
